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Effect of mopidamol on survival in carcinoma of the lung and colon: Final report of veterans administration cooperative study no. 188

  • Leo R. Zacharski
  • , Thomas E. Moritz
  • , Linda A. Baczek
  • , Frederick R. Rickles
  • , Richard L. Edwards
  • , Walter B. Forman
  • , R. Jackson Forcier
  • , C. J. Cornell
  • , Clair M. Haakenson
  • , Harold S. Ballard
  • , Edward D. Crum
  • , Gerhard J. Johnson
  • , James Levine
  • , Waun Ki Hong
  • , Joseph F. O'donnell
  • , Richard L. Schilsky
  • , Q. Scott Ringenberg
  • , Francisco Robert
  • , Monica B. Spaulding
  • , Karl Tornyos
  • Charles Williams, Stanley Zucker, Charles S. Faulkner, Walter L. Eaton, Charles L. Hoppel
  • Department of Veterans Affairs
  • Dartmouth College
  • VA Medical Center
  • University of Connecticut
  • Vincent Charity Hospital and Health Center
  • Columbia University
  • Case Western Reserve University
  • University of Minnesota Twin Cities
  • Boston University
  • University of Puerto Rico
  • Tulane University
  • University of South Florida
  • Stony Brook University

Research output: Contribution to journalArticlepeer-review

51 Scopus citations

Abstract

Mopidamol (RA-233), a derivative of dipyridamole, is a phosphodiesterase inhibitor that has been shown previously to limit progression of malignancy in certain experimental animal models and in a pilot study in humans. RA-233 plus chemotherapy was compared with chemotherapy alone in a 5-year double-blind trial involving 719 patients with advanced carcinomas of the lung and of the colon. RA-233 treatment was associated with a statistically significant prolongation of survival in patients with non-small cell lung cancer (N-SCLC) limited to one hemithorax and with reduction in mean plasma fibrogen concentration. RA-233 was not toxic. The favorable effects on survival could not be explained by any factor other than the RA-233 treatment. In other tumor categories tested, no differences in survival were observed. These results suggest that RA-233 is useful in the treatment of N-SCLC of limited extent. They also suggest that therapeutic intervention aimed at modified intracellular pathways might constitute a novel investigative approach to the treatment of cancer.

Original languageEnglish
Pages (from-to)90-97
Number of pages8
JournalJournal of the National Cancer Institute
Volume80
Issue number2
DOIs
StatePublished - Mar 16 1988

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